Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Propargyl alcohol → (3-Phenyl-5-isoxazolyl)methanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Propargyl alcohol | HCID 7859 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | (Z)-Benzaldehyde oxime | HCID 12143 | — |
| 반응물 | Chlorosuccinimide | HCID 31398 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (3-Phenyl-5-isoxazolyl)methanol | HCID 2763417 | 76.8% |
반응 단계
10.0 mmol of benzaldehyde oxime and 30 mL of dry dichloromethane were placed in a 250 mL single-necked round-bottom flask. 1.60 g (12.0 mmol) of N-chlorosuccinimide (NCS) was added under stirring. After NCS was completely dissolved by slightly heating, 0.56 g (10.0 mmol) of 2-propyn-1-ol was added dropwise, and then 20 mL solution of 10.1 g (10.0 mmol) of triethylamine in dichloromethane. After the addition was complete, the system was refluxed. After the completion of the reaction monitored by TLC, the mother liquor was washed with water, dried over anhydrous sodium sulfate, and separated by column chromatography (Vpetroleum ether:Vethyl acetate=5:1-2:1) to give 3-phenyl-5-hydroxymethyl-isoxazole in 76.8% yield.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09193718B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-5429e1783feb4fff95493802e03cf19a |
| 출처 메모 | uspto-grants-2015_11 |